Gastroenterology Flashcards
dDx vomiting infant
Pyloric stenosis GORD Possetting Gastroenteritis Small bowel obstruction Systemic/localised infection Hirshsprungs Oesophageal fistula Galactosaemia
dDx vomiting adolescent
Raised ICP
Migraine
Bulimia
Pregnancy (test all girls >12y)
Features pyloric stenosis
Characterised by gradual thickening of the pyloric muscles
More common in boys and first borns
Typically non-bilious vomiting at 2-8 weeks
Progressive frequency and forcefulness resulting in projectile vomiting following feeds
Loss of interest in feeds
Palpable pyloric mass in RUG with a full stomach
Visible gastric peristalsis from left to right
Hypochloremia, hypokalemic alkalosis, with increased bicarbonate
US pyloric stenosis
hypertrophy: thickness >4mm; length >18mm; failure fluid passage beyond pylorus
Mx Pyloric stenosis
Correct dehydration and electrolyte imbalances
Definitive treatment is myomectomy via RUQ or supraumbilical incision.
Normal feeding resumes after 6 hours
Features GORD
Typically following feeds, arching back, worse lying down after feeds, better sitting up
Address feeding techniques and positioning
Associated with cerebral palsy and neurodevelopmental disorder
Mx GORD
Thickening of feeds ,e,g, gaviscon
Acid suppression .e.g. Ranitidine, omeprazole
In severe cases surgery may be indicated- Nissens procedure high failure
Features possetting
Non-forceful regurgitation, milky vomit, low volumes
Parental reassurance
Features gastroenteritis
Inflammation of the bowel secondary to infection
Typically rotavirus in children: now on immunisation schedule
Sudden onset diarrhea and vomiting, typically affected contacts, weight loss, poor feeding
Cx gastroenteritis
Post gastritis syndrome: watery diarrhoea on reintroduction of normal diet, initiate oral rehydration
Mx gastroenteritis
Stool culture if immunocompromised, blood/mucus in stool or evidence of sepsis
Oral rehydration solution and isolation to limit spread
Features small bowel obstruction
May be recognised antenatally
Persistent bile stained vomiting and increasing prominent abdominal distention
Initial passage of meconium and no further stool
Features duodenal atresia
Commonly associated with down’s syndrome and congenital malformations
Double bubble on X Ray
Mx dudodenal atresia
NG decompression
Surgical correction
Features jejunum/ileum atresia
secondary to vascular occlusion in utero
may include multiple atretic segments
Features malrotation
Abnormal rotation during development
DJ flexure on right of midline
Volvulus formed when mesentery twists on own axis leading to vascular compromise and mechanical obstruction
Diagnosis by upper GI contrast
Mx malrotation
Ladd’s procedure to correct and removal of appendix to prevent later confusion with appendicitis
Features meconium ileus
Thickened impacted meconium in lower ileum
Commonly in cystic fibrosis
Mx meconium ileus
Enema and rectal washout
Laparotomy with temporary ileostomy
Features hirschsprungs
Absence of ganglion cells in mesenteric and submucosal plexus
Neonatal presentation as failure/delay in meconium passage
Abdominal distention, bile stained vomiting
Release of flatus and stool with PR examination
Mx hirschsprungs
Rectal biopsy shows absence of ganglion cells with large ACh positive nerve trunks
Definitive management: colostomy with anastomosis normally innervated bowel to the anus
Features oesophageal fistula
Persistent salivation, drooling, coughing and choking, especially when fed
Associated with VACTERL abnormalities
High risk of aspiration